Disease #01596 (CMH1 (cardiomyopathy, hypertrophic, familial, type 1), OMIM:192600)

Official abbreviation CMH1
Name cardiomyopathy, hypertrophic, familial, type 1
OMIM ID 192600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Digenic dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 3 genes CAV3, MYH7, MYLK2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-10-01 20:50:48 +02:00 (CEST)


Individuals

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00436735 family PubMed: Franke 2024, Journal: Franke 2024 5-generation-family, 10 affected (7F, 3M) and 4 sudden cardiac death (generations 1 and 2) F - Poland - - - - - CMH1 CMH MYH7 MYH7 1 10 Dorota Czapczak
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